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TWI824665B - Adhesive film for wafer back grinding - Google Patents

Adhesive film for wafer back grinding Download PDF

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Publication number
TWI824665B
TWI824665B TW111130484A TW111130484A TWI824665B TW I824665 B TWI824665 B TW I824665B TW 111130484 A TW111130484 A TW 111130484A TW 111130484 A TW111130484 A TW 111130484A TW I824665 B TWI824665 B TW I824665B
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adhesive
particles
base material
wafer
layer
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TW202306759A (en
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鄭喆
高乾英
崔裁原
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韓商利諾士尖端材料有限公司
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J4/00Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/04Non-macromolecular additives inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/06Non-macromolecular additives organic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • C09J7/25Plastics; Metallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
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    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/29Laminated material
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38Pressure-sensitive adhesives [PSA]
    • H10P72/7402
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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    • C09J2203/00Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/326Applications of adhesives in processes or use of adhesives in the form of films or foils for bonding electronic components such as wafers, chips or semiconductors
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/30Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/312Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Engineering & Computer Science (AREA)
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  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Manufacturing & Machinery (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Polishing Bodies And Polishing Tools (AREA)
  • Mechanical Treatment Of Semiconductor (AREA)

Abstract

An adhesive film for wafer back grinding is provided in the present invention. The adhesive film for wafer back grinding comprises: a multilayer substrate including an upper base material layer and a lower base material layer; a first adhesive layer disposed on the upper base material layer; and a second adhesive layer disposed between the upper base material layer and the lower base material layer. The second adhesive layer is formed of an adhesive composition comprising a light-transmitting adhesive resin and light scattering particles, and the second adhesive layer satisfies the following formula 1. The refractive index of the above-mentioned light scattering particles is 1.42 to 1.60, which reduce or suppress the generation of adhesive residues in the back grinding process of the wafer, and has an excellent buffering effect on the surface of the wafer, and also improves the uniformity of wafer thickness after the back grinding process. Formula 1: 0.05≤|A-B|≤0.2, wherein A is the refractive index of the light-transmitting adhesive resin, and B is the refractive index of the light scattering particles.

Description

晶圓背面研磨用黏結膜Adhesive film for wafer backside grinding

本發明涉及黏結膜,在晶圓的背面研磨((晶圓背面研磨(wafer back grinding)或晶圓磨薄(wafer lapping)或晶圓減薄(wafer thinning))製程中,為了保護晶圓的表面而使用。更具體地,本發明涉及如下的晶圓背面研磨用黏結膜,即,在進行晶圓背面研磨加工後,在消除黏結膜(剝離)時通過減少或消除黏結劑的殘留物(residue)的產生使得加工性非常優秀。 The present invention relates to an adhesive film, which is used to protect the wafer during the back grinding (wafer back grinding) or wafer lapping (wafer thinning) process. Used on the surface. More specifically, the present invention relates to an adhesive film for wafer back grinding that is used by reducing or eliminating the residue of the adhesive when removing (peeling off) the adhesive film after performing a wafer back grinding process ( The production of residue) makes the processability very excellent.

隨著近年來技術的發展,要求半導體芯片的小型化、高密度化及薄型化,因此,晶圓也要求薄型化。用於薄型化晶圓芯片的典型方法是通過研磨晶圓的背面來減少厚度,可根據使用半導體芯片的電子裝置的種類或規格來進行研磨製程,從而實現晶圓的薄型化。 With the development of technology in recent years, semiconductor chips are required to be smaller, denser, and thinner. Therefore, wafers are also required to be thinner. A typical method for thinning a wafer chip is to reduce the thickness by grinding the backside of the wafer. The grinding process can be performed according to the type or specification of the electronic device using the semiconductor chip to achieve thinning of the wafer.

由於半導體芯片的晶圓的背面研磨是施加物理衝擊的過程,因此為了保護晶圓的表面,通常在黏附晶圓背面研磨用黏結膜的狀態下進行晶圓的背面研磨。這種黏結膜包括基材和用於黏結晶圓表面的黏結層,為了緩衝效果,通常在基材背面形成緩衝層或衝擊吸收層。並且,黏結層通常由能量射線固化黏結組合物形成。 Since the back grinding of a semiconductor chip wafer is a process of applying physical impact, in order to protect the surface of the wafer, the back grinding of the wafer is usually performed with an adhesive film for wafer back grinding attached. This adhesive film includes a base material and an adhesive layer used to bond the wafer surface. For buffering effect, a buffer layer or impact-absorbing layer is usually formed on the back of the base material. Furthermore, the adhesive layer is usually formed of an energy ray curable adhesive composition.

並且,在進行晶圓的背面研磨後,為了從晶圓表面去除晶圓背面研磨製程用黏結膜,通過照射能量射線來降低黏結力並剝離。 Furthermore, in order to remove the adhesive film used in the wafer back polishing process from the wafer surface after back polishing the wafer, energy rays are irradiated to reduce the adhesive force and peel off.

另一方面,隨著近年來訊息通訊技術的飛速發展和市場的擴大,對於半導體裝置的需求逐漸高密度化。由此,配置於晶圓表面上的有源層(active layer)的厚度增加,有源層的凹凸(或圖案)也逐漸增大。因此,當剝離晶圓背面研磨用黏結膜時,在由於有源層的凹凸而產生的陰影區域中,發生能量射線固化沒有充分進行的情況。其結果,由於晶圓背面研磨用黏結膜的黏結力沒有充分降低,使得剝離力降低,因此來源於黏結膜的黏結劑殘留物容易殘留在晶圓表面,阻礙加工性,最終對製備的半導體芯片的品質產生不利的影響,並且存在用於解決該問題的技術要求。 On the other hand, with the rapid development of information communication technology and market expansion in recent years, the demand for semiconductor devices has gradually increased in density. As a result, the thickness of the active layer (active layer) disposed on the wafer surface increases, and the unevenness (or pattern) of the active layer also gradually increases. Therefore, when the adhesive film for wafer back polishing is peeled off, energy beam curing may not fully proceed in the shadow area caused by the unevenness of the active layer. As a result, since the adhesive force of the adhesive film used for wafer back grinding is not sufficiently reduced, the peeling force is reduced. Therefore, adhesive residue derived from the adhesive film easily remains on the wafer surface, hindering processability, and ultimately affecting the prepared semiconductor chip. quality is adversely affected, and there are technical requirements to address the problem.

本發明的目的在於,提供一種晶圓背面研磨用黏結膜,即使在晶圓或晶圓表面的有源層存在較大的凹凸部分,在晶圓背面研磨製程後,當剝離晶圓背面研磨用黏結膜時,也可減少或抑制黏結劑殘留物的產生。 The object of the present invention is to provide an adhesive film for wafer back grinding. Even if there are large uneven portions on the wafer or the active layer on the wafer surface, after the wafer back grinding process, when the wafer back grinding adhesive film is peeled off, When bonding the film, it can also reduce or inhibit the generation of adhesive residue.

本發明的目的並不限定於以上所提及的目的,未提及的本發明的其他目的及優點可通過如下說明來理解,可通過本發明實施例來更清楚地理解。並且,可知本發明的目的及優點可通過發明要求保護範圍中所示的方案及其組合來實現。 The object of the present invention is not limited to the above-mentioned objects. Other objects and advantages of the present invention that are not mentioned can be understood through the following description and can be understood more clearly through the embodiments of the present invention. Furthermore, it can be seen that the objects and advantages of the present invention can be achieved by the solutions and combinations thereof shown in the scope of the claimed invention.

為了解決上述的技術問題,根據本發明的一實施方式,可提供一種晶圓背面研磨用黏結膜,其特徵在於,包括:多層基材,包括上部基材層及下部基材層;第一黏結層,配置於上述上部基材層上;以及第二黏結層,配置於上述上部基材層與下部基材層之間,上述第二黏結層由包含透光性黏結樹脂及光散射粒子的黏結組合物形成,並滿足如下式1,上述光散射粒子的折射率為1.42~1.60。 In order to solve the above technical problems, according to an embodiment of the present invention, an adhesive film for wafer backside grinding can be provided, which is characterized in that it includes: a multi-layer base material, including an upper base material layer and a lower base material layer; a first adhesive film layer, disposed on the above-mentioned upper base material layer; and a second adhesive layer, disposed between the above-mentioned upper base material layer and the lower base material layer, the above-mentioned second adhesive layer is composed of an adhesive layer containing a translucent adhesive resin and light scattering particles. A composition is formed and satisfies the following formula 1. The refractive index of the above light scattering particles is 1.42~1.60.

Figure 111130484-A0305-02-0005-7
Figure 111130484-A0305-02-0005-7

在上述式1中,A是透光性黏結樹脂的折射率,B是光散射粒子的折射率。 In the above formula 1, A is the refractive index of the translucent binder resin, and B is the refractive index of the light scattering particles.

相對於100重量份的上述第二黏結層的黏結組合物,可包含0.1重量份至10重量份的上述光散射粒子。 The above-mentioned light scattering particles may be included in 0.1 to 10 parts by weight relative to 100 parts by weight of the above-mentioned adhesive composition of the second adhesive layer.

上述光散射粒子可包含無機粒子及有機粒子中的一種以上。 The light scattering particles may include at least one type of inorganic particles and organic particles.

上述光散射粒子的平均粒徑可以為1μm~50μm。 The average particle diameter of the above-mentioned light scattering particles may be 1 μm ~ 50 μm.

上述無機粒子可包含選自由二氧化矽粒子、玻璃粉及石英粒子組成的組中的一種以上。 The inorganic particles may include at least one selected from the group consisting of silica particles, glass powder, and quartz particles.

上述有機粒子可包含選自由丙烯酸樹脂粒子、聚苯乙烯樹脂粒子、苯乙烯-丙烯酸共聚物成分的粒子、聚乙烯樹脂粒子、環氧樹脂粒子、矽樹脂粒子、聚偏氟乙烯粒子、聚四氟乙烯粒子、二乙烯基苯樹脂粒子、苯酚樹脂粒子、氨基甲酸乙酯樹脂粒子、醋酸纖維素粒子、尼龍粒子、纖維素粒子、苯代三聚氰胺樹脂粒子及三聚氰胺樹脂粒子組成的組中的一種以上。 The above-mentioned organic particles may include particles selected from the group consisting of acrylic resin particles, polystyrene resin particles, styrene-acrylic acid copolymer components, polyethylene resin particles, epoxy resin particles, silicone resin particles, polyvinylidene fluoride particles, and polytetrafluoroethylene. One or more of the group consisting of ethylene particles, divinylbenzene resin particles, phenol resin particles, urethane resin particles, cellulose acetate particles, nylon particles, cellulose particles, benzinated melamine resin particles and melamine resin particles.

本發明的晶圓背面研磨用黏結膜的總透光率可以為70%以上,漫透射率可以為6%以上。 The total light transmittance of the adhesive film for wafer backside grinding of the present invention can be more than 70%, and the diffuse transmittance can be more than 6%.

上述第一黏結層的厚度可以為10μm~100μm,上述第二黏結層的厚度可以為10μm~100μm。 The thickness of the above-mentioned first adhesive layer may be 10 μm~100 μm, and the thickness of the above-mentioned second adhesive layer may be 10 μm~100 μm.

上述下部基材層及上部基材層分別可包含選自由聚對苯二甲酸乙二醇酯、聚萘二甲酸乙二醇酯、聚對苯二甲酸丁二酯、全芳族聚酯、聚醯亞胺、聚醯胺、聚碳酸酯、聚縮醛、改性聚苯醚、聚苯硫醚、聚碸、聚醚酮及雙向拉伸聚丙烯組成的組中的一種以上,較佳地,下部基材層及上部基材層可由聚對苯二甲酸乙二醇酯形成。 The above-mentioned lower base material layer and the upper base material layer may respectively comprise polyethylene terephthalate, polyethylene naphthalate, polybutylene terephthalate, fully aromatic polyester, poly One or more of the group consisting of imine, polyamide, polycarbonate, polyacetal, modified polyphenylene ether, polyphenylene sulfide, polystyrene, polyetherketone and biaxially oriented polypropylene, preferably , the lower base material layer and the upper base material layer may be formed of polyethylene terephthalate.

上述第一黏結層可由包含丙烯酸類黏結樹脂的黏結組合物形成。 The first adhesive layer may be formed of an adhesive composition including an acrylic adhesive resin.

上述第二黏結層的上述透光性黏結樹脂可包含透光性丙烯酸類黏結樹脂。 The translucent adhesive resin of the second adhesive layer may include translucent acrylic adhesive resin.

在30℃的溫度條件下的上述第二黏結層的剪切儲能模量可以為0.05MPa~5.00MPa。 The shear storage modulus of the above-mentioned second adhesive layer under the temperature condition of 30°C may be 0.05MPa~5.00MPa.

在上述上部基材層的上部面、上述上部基材層的下部面及上述下部基材層的上部面中的至少一面還可包括底漆層。 A primer layer may be further provided on at least one of the upper surface of the upper base material layer, the lower surface of the upper base material layer, and the upper surface of the lower base material layer.

當將本發明的晶圓背面研磨用黏結膜適用於背面研磨製程時,即使在晶圓或晶圓表面的有源層存在較大的凹凸部分,也可在黏附於晶圓表面時具有優秀的凹凸埋入性,在晶圓背面研磨製程後,當剝離晶圓背面研磨用黏結膜時,可通過減少或抑制黏結劑殘留物的產生來提高晶圓處理工藝性及製備的半導體芯片的品質。 When the adhesive film for wafer back grinding of the present invention is applied to the back grinding process, even if there are large uneven portions on the wafer or the active layer on the wafer surface, it can have excellent adhesion to the wafer surface. Concave-convex embedding properties can improve the wafer processing process and the quality of the prepared semiconductor chips by reducing or inhibiting the generation of adhesive residues when peeling off the adhesive film for wafer back grinding after the wafer back grinding process.

並且,當將本發明的晶圓背面研磨用黏結膜適用於背面研磨製程時,可對晶圓的表面(表面)的緩衝效果(或保護效果)優秀,並且也可在背面研磨製程後提高晶圓的厚度的均勻性。 Furthermore, when the adhesive film for wafer back grinding of the present invention is applied to the back grinding process, it can have an excellent buffering effect (or protective effect) on the surface of the wafer, and can also improve the wafer strength after the back grinding process. Uniformity of thickness of circle.

本說明書的效果並不限定於以上所提及的效果,未提及的其他效果可由本領域中具有通常知識者從如下的記載中清楚地理解。以下,將在描述用於實施本發明的具體細節的同時描述上述效果和本發明的具體效果。 The effects of this specification are not limited to the effects mentioned above, and other effects not mentioned can be clearly understood by those with ordinary knowledge in the art from the following description. Hereinafter, the above effects and specific effects of the present invention will be described while describing specific details for implementing the present invention.

10:第一黏結層 10: First adhesive layer

20:上部基材層 20: Upper base material layer

30:第二黏結層 30:Second adhesive layer

40:下部基材層 40: Lower base material layer

100:晶圓背面研磨用黏結膜 100: Adhesive film for wafer backside grinding

200:背面研磨製程前的晶圓 200: Wafer before back grinding process

210:背面研磨製程後的晶圓 210: Wafer after back grinding process

300:有源層 300:Active layer

S1-S5:步驟 S1-S5: Steps

P:光散射粒子 P: light scattering particles

R:黏結劑的殘留物殘留區域 R: Residue area of adhesive

圖1簡要示出將本發明的一實施方式的晶圓背面研磨用黏結膜適用於晶圓背面研磨製程及之後的剝離過程的流程圖。 FIG. 1 schematically shows a flow chart of applying an adhesive film for wafer back polishing according to an embodiment of the present invention to a wafer back polishing process and a subsequent peeling process.

圖2示出本發明的一實施方式的晶圓背面研磨用黏結膜的剖視圖。 FIG. 2 shows a cross-sectional view of an adhesive film for wafer backside polishing according to one embodiment of the present invention.

將參照附圖對前述的目的、特徵及優點進行詳細說明,由此,本發明所屬技術領域的通常知識者可容易地實施本發明的技術思想。在說明本發明的過程中,若判斷為對與本發明相關的公知技術的具體說明可能不必要地混淆本發明的主旨,則省略詳細說明。如下,參照附圖,對本發明的較佳實施例進行詳細的說明。在附圖中,相同的附圖標記用於表示相同或類似的結構要素。 The aforementioned objects, features, and advantages will be described in detail with reference to the accompanying drawings, whereby those of ordinary skill in the technical field to which the present invention belongs can easily implement the technical idea of the present invention. In describing the present invention, if it is judged that a detailed description of a known technology related to the present invention may unnecessarily obscure the gist of the present invention, the detailed description will be omitted. As follows, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. In the drawings, the same reference numbers are used to represent the same or similar structural elements.

在本說明書中,任意結構配置於結構要素的“上部(或下部)”或結構要素的“上(或下)”不僅意味著任意結構與上述結構要素的上部面(或下部面)相接觸的配置,還意味著其他結構可介於上述結構要素與配置於上述結構要素上(或下)的任意結構之間。 In this specification, any structure arranged "upper (or lower)" of a structural element or "upper (or lower)" of a structural element does not only mean that any structure is in contact with the upper surface (or lower surface) of the above structural element. Arrangement also means that other structures can be interposed between the above-mentioned structural elements and any structure arranged on (or below) the above-mentioned structural elements.

除非本說明書中另有明確的提及,否則在本說明書中所使用的單數表達包括複數表達。在本申請中,“由......組成”或“包括”等術語不應被解釋為必須包括說明書中記載的所有各種結構要素,應解釋為可不包括其中部分結構要素,或還可包括額外的結構要素。 Unless otherwise expressly mentioned in this specification, singular expressions used in this specification include plural expressions. In this application, terms such as "consisting of" or "includes" should not be interpreted as necessarily including all the various structural elements recorded in the specification, but should be interpreted as not including some of the structural elements, or may also include Includes additional structural elements.

在本說明書中,“一側面”、“另一側面”、“兩側面”等術語用於區分某個結構要素與其他結構要素,結構要素並不受限於上述術語。 In this specification, terms such as "one side", "the other side", and "both sides" are used to distinguish a certain structural element from other structural elements, and structural elements are not limited to the above terms.

本說明書的記載中,“(甲基)丙烯酸酯”是作為包含“丙烯酸酯”及“甲基丙烯酸酯”的術語而使用,對於與其類似的術語也相同。 In the description of this specification, "(meth)acrylate" is used as a term including "acrylate" and "methacrylate", and the same applies to similar terms.

以下,在說明本發明的過程中,省略對不必要地混淆本發明的主旨的相關的公知技術的詳細說明。 In the following description of the present invention, detailed descriptions of related known technologies that may unnecessarily obscure the gist of the present invention will be omitted.

圖1示例性的示出將本發明一實施方式的晶圓背面研磨用黏結膜100適用於晶圓,在背面研磨之後通過照射能量射線來降低黏結力剝離的製程的流程圖。 FIG. 1 schematically illustrates a flow chart of a process in which an adhesive film 100 for wafer back polishing according to an embodiment of the present invention is applied to a wafer, and the adhesive film is peeled off by irradiating energy rays after back polishing.

具體地,圖1的S1是在晶圓背面研磨製程前的準備晶圓的步驟(裝載晶圓),示出有源層300配置於晶圓200的表面,上述有源層300可包括存在於晶圓表面的凹凸(圖案)的基材層。 Specifically, S1 in FIG. 1 is the step of preparing the wafer (loading the wafer) before the wafer back grinding process. It shows that the active layer 300 is disposed on the surface of the wafer 200. The active layer 300 may include The base material layer of the unevenness (pattern) on the wafer surface.

圖1的S2是將本發明的晶圓背面研磨用黏結膜100黏附(或貼附)在晶圓的表面側的步驟,由此,在背面研磨時起到保護晶圓200的表面和/或有源層300的作用。 S2 in FIG. 1 is a step of adhering (or attaching) the adhesive film 100 for wafer back grinding of the present invention to the surface side of the wafer, thereby protecting the surface of the wafer 200 during back grinding and/or The role of active layer 300.

圖1的S3簡要示出了進行背面研磨製程的步驟,在背面研磨製程中,可不受限制地使用在本技術領域中使用的多種背面研磨設備,例如,可使用在承載盤(chuck table)上裝載(loading)晶圓後可旋轉砂輪(grinding wheel)的設備。另一方面,在背面研磨製程前的晶圓的厚度大約在700μm~900μm的範圍,在背面研磨製程後, 根據適用半導體芯片的電子設備的規格,最終晶圓的厚度可薄型化到大約30μm~300μm的範圍。 S3 of Figure 1 briefly illustrates the steps of performing a back grinding process. In the back grinding process, a variety of back grinding equipment used in this technical field can be used without limitation, for example, it can be used on a chuck table. Equipment that can rotate the grinding wheel after loading the wafer. On the other hand, the thickness of the wafer before the back grinding process is approximately in the range of 700μm~900μm. After the back grinding process, Depending on the specifications of the electronic equipment to which semiconductor chips are applied, the thickness of the final wafer can be reduced to a range of approximately 30 μm to 300 μm.

圖1的S4簡要示出在背面研磨製程後為了剝離晶圓背面研磨用黏結膜100照射能量射線(典型的是紫外線(UV))的步驟,相對於背面研磨製程前的晶圓200,背面研磨製程後的晶圓210的厚度減少。由此,晶圓背面研磨用黏結膜100的黏結層通常由能量射線固化黏結組合物形成。 S4 of FIG. 1 schematically shows the step of irradiating energy rays (typically ultraviolet (UV)) in order to peel off the adhesive film 100 for back grinding of the wafer after the back grinding process. Compared with the wafer 200 before the back grinding process, the back grinding The thickness of the wafer 210 after the process is reduced. Therefore, the adhesive layer of the adhesive film 100 for wafer back polishing is usually formed of an energy ray curable adhesive composition.

圖1的S5簡要示出了在背面研磨製程後剝離晶圓背面研磨用黏結膜100的步驟。在此情況下,若到達晶圓背面研磨用黏結膜100的能量射線的曝光不足,則黏結力不能充分地降低至能夠良好地剝離的程度,因此,在剝離步驟中可能會殘留晶圓背面研磨用黏結膜100的殘留物。如上所述,在圖1中例示性的表示了黏結劑的殘留物殘留區域(R)。 S5 in FIG. 1 briefly illustrates the step of peeling off the adhesive film 100 for wafer backside polishing after the backside polishing process. In this case, if the exposure of energy rays reaching the adhesive film 100 for wafer back polishing is insufficient, the adhesive force cannot be sufficiently reduced to the extent that good peeling is possible, and therefore the wafer back grinding may remain in the peeling step. Use the residue of Adhesive Film 100. As mentioned above, FIG. 1 illustrates the adhesive residue remaining area (R).

若在晶圓上殘留晶圓背面研磨用黏結膜100的殘留物,則可產生對工藝性及製備的半導體芯片的品質產生不利的影響的問題。並且,由於隨著配置於晶圓200或晶圓表面的有源層300的凹凸(圖案)程度越深,能量射線達不到的陰影區域會越增加,因此上述問題進一步深化。 If residues of the adhesive film 100 for wafer back polishing remain on the wafer, problems may arise that may adversely affect processability and the quality of the semiconductor chip produced. Furthermore, as the degree of unevenness (pattern) of the active layer 300 disposed on the wafer 200 or the wafer surface becomes deeper, the shadow areas that cannot be reached by energy rays increase, so the above problem is further deepened.

本發明人著眼於如上所述的問題,為了使能量射線的曝光能夠充分達到晶圓背面研磨用黏結膜,在晶圓背面研磨用黏結膜100的第二黏結層30中添加了光散射粒子P。 The inventor of the present invention focused on the above-mentioned problems, and in order to allow the exposure of energy rays to fully reach the adhesive film for wafer back polishing, light scattering particles P were added to the second adhesive layer 30 of the adhesive film for wafer back polishing 100 .

像這樣,由於上述第二黏結層30由包含透光性黏結樹脂及光散射粒子P的黏結組合物形成,所以可表現出光散射效果。因此,可將照射的能量射線均勻地分散在晶圓背面研磨用黏結膜100,發現了可以解決上述的曝光不足的問題,並完成了本發明。 In this way, since the second adhesive layer 30 is formed of an adhesive composition including a translucent adhesive resin and light scattering particles P, it can exhibit a light scattering effect. Therefore, it was found that the irradiated energy rays can be uniformly dispersed in the adhesive film 100 for wafer back polishing, and the above-mentioned problem of insufficient exposure can be solved, and the present invention was completed.

因此,如圖2所示,本發明的晶圓背面研磨用黏結膜具有如下的結構,其包括:多層基材,包括上部基材層20及下部基材層40;第一黏結層10,配置於上述上部基材層20上;以及第二黏結層30,配置於上述上部基材層20及下部基材層40之間,上述第二黏結層30可由包含透光性黏結樹脂及光散射粒子P的黏結組合物形成。 Therefore, as shown in Figure 2, the adhesive film for wafer backside grinding of the present invention has the following structure, which includes: a multi-layer base material, including an upper base material layer 20 and a lower base material layer 40; a first adhesive layer 10 configured on the upper base material layer 20; and a second adhesive layer 30 disposed between the upper base material layer 20 and the lower base material layer 40. The second adhesive layer 30 can be made of a translucent adhesive resin and light scattering particles. The adhesive composition of P is formed.

以下,對晶圓背面研磨用黏結膜的特性及各層的結構進行詳細說明。 Below, the characteristics of the adhesive film for wafer backside polishing and the structure of each layer are described in detail.

多層基材 multilayer substrate

多層基材包括下部基材層40、上部基材層20及第二黏結層30。第一黏結層10配置於上部基材層20上,第二黏結層30配置於下部基材層40與上部基材層20之間。在本發明的晶圓背面研磨用黏結膜中,多層基材具有第二黏結層30配置於下部基材層40與上部基材層20之間的三明治結構。 The multi-layer substrate includes a lower substrate layer 40 , an upper substrate layer 20 and a second adhesive layer 30 . The first adhesive layer 10 is arranged on the upper base material layer 20 , and the second adhesive layer 30 is arranged between the lower base material layer 40 and the upper base material layer 20 . In the adhesive film for wafer back polishing of the present invention, the multilayer base material has a sandwich structure in which the second adhesive layer 30 is arranged between the lower base material layer 40 and the upper base material layer 20 .

下部基材層40及上部基材層20可由具有高拉伸彈性模量的材料形成。更具體地,下部基材層40及上部基材層20可具有1000MPa以上的拉伸彈性模量,例如1200MPa以上、1500MPa以上、2000MPa以上、3000MPa以上,在此情況下的拉伸彈性模量以在23℃的溫度條件下的測定值為基準。 The lower base material layer 40 and the upper base material layer 20 may be formed of a material with a high tensile elastic modulus. More specifically, the lower base material layer 40 and the upper base material layer 20 may have a tensile elastic modulus of 1000 MPa or more, such as 1200 MPa or more, 1500 MPa or more, 2000 MPa or more, 3000 MPa or more. In this case, the tensile elastic modulus is The measured value under the temperature condition of 23°C is the basis.

當下部基材層40及上部基材層20的拉伸彈性模量相對較低,小於1000MPa時,由於對晶圓或半導體芯片的支撐力較低,因此有可能在背面研磨製程(背磨製程)中產生半導體芯片的碰撞。 When the tensile elastic modulus of the lower base material layer 40 and the upper base material layer 20 is relatively low, less than 1000 MPa, due to the low support force for the wafer or semiconductor chip, it is possible to perform the back grinding process (back grinding process). ) produces a collision of semiconductor chips.

下部基材層40及上部基材層20分別可包含選自由聚對苯二甲酸乙二醇酯(PET)、聚萘二甲酸乙二醇酯(PEN)、聚對苯二甲酸丁二酯(PBT)、全芳族聚酯等的聚醯亞胺(PI)、聚醯胺(PA)、聚碳酸酯(PC)、聚縮醛、改性聚苯醚、聚苯硫醚、聚碸、聚醚酮及雙向拉伸聚丙烯(Oriented Poly-propylene)組成的組中的一種以上。 The lower base material layer 40 and the upper base material layer 20 may respectively comprise polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polybutylene terephthalate ( PBT), fully aromatic polyester and other polyimide (PI), polyamide (PA), polycarbonate (PC), polyacetal, modified polyphenylene ether, polyphenylene sulfide, polypropylene, One or more of the group consisting of polyetherketone and biaxially oriented polypropylene (Oriented Poly-propylene).

並且,下部基材層40及上部基材層20可以由相同的材料形成,例如,下部基材層40及上部基材層20可以由聚對苯二甲酸乙二醇酯(PET)材料形成。 Furthermore, the lower base material layer 40 and the upper base material layer 20 may be formed of the same material. For example, the lower base material layer 40 and the upper base material layer 20 may be formed of polyethylene terephthalate (PET) material.

對下部基材層40及上部基材層20的厚度沒有特別限定,可具有相同的厚度。例如,下部基材層40及上部基材層20可分別具有約10μm~150μm的厚度。另一方面,在本發明中,由於下部基材層40及上部基材層20可具有高拉伸彈性模量,當下部基材層40及上部基材層20,尤其是上部基材層20的厚度過厚時,可能會容易受到背面研磨製程中產生的衝擊。因此,例如,下部基材層40及上部基材層20的厚度可以為約150μm以下,但並不限定於此。 The thickness of the lower base material layer 40 and the upper base material layer 20 is not particularly limited, and they may have the same thickness. For example, the lower base material layer 40 and the upper base material layer 20 may each have a thickness of about 10 μm ~ 150 μm. On the other hand, in the present invention, since the lower base material layer 40 and the upper base material layer 20 can have high tensile elastic modulus, when the lower base material layer 40 and the upper base material layer 20 , especially the upper base material layer 20 If the thickness is too thick, it may be susceptible to impact during the back grinding process. Therefore, for example, the thickness of the lower base material layer 40 and the upper base material layer 20 may be about 150 μm or less, but is not limited thereto.

另一方面,根據下部基材層40和/或上部基材層20的需要,可包括少量的各種添加劑,如耦合劑、可塑劑、防靜電劑、抗氧化劑等。 On the other hand, according to the needs of the lower base material layer 40 and/or the upper base material layer 20, a small amount of various additives, such as coupling agent, plasticizer, antistatic agent, antioxidant, etc., may be included.

第一黏結層 first bonding layer

在圖2中第一黏結層10是與晶圓黏結(或黏附)的部分。第一黏結層10只要是在常溫條件下具有適當的黏結性就沒有特別限定,可由作為公知的紫外線(UV)固化黏結組合物的丙烯酸類黏結組合物、矽類黏結組合物、聚酯類黏結組合物、聚醯胺類黏結組合物、氨基甲酸乙酯黏結組合物、苯乙烯-二烯嵌段共聚物黏結組合物等的多種黏結組合物形成,較佳地,可由丙烯酸類黏結組合物形成。 In FIG. 2 , the first adhesive layer 10 is the part that is bonded (or adhered) to the wafer. The first adhesive layer 10 is not particularly limited as long as it has appropriate adhesiveness under normal temperature conditions. It can be made of an acrylic adhesive composition, a silicon adhesive composition, a polyester adhesive composition, which are known ultraviolet (UV) curing adhesive compositions. It is formed from various adhesive compositions such as polyamide adhesive composition, urethane adhesive composition, styrene-diene block copolymer adhesive composition, etc. Preferably, it can be formed from an acrylic adhesive composition. .

例如,第一黏結層10可由包含丙烯酸類黏結樹脂的黏結組合物形成,丙烯酸類黏結樹脂可以是具有碳原子數為1至14的烷基的(甲基)丙烯酸類單體的聚合物,具體地,可以是選擇由丙烯酸乙基己酯、丙烯酸丁酯、丙烯酸乙酯、丙烯酸甲酯、丙烯酸、丙烯酸羥乙酯及丙烯酸羥丁酯組成的組中的一種以上的聚合物,較佳地,可以是包含單體聚合的聚合物,上述單體包括與羧基或羥基鍵和的單體。 For example, the first adhesive layer 10 may be formed of an adhesive composition including an acrylic adhesive resin. The acrylic adhesive resin may be a polymer of a (meth)acrylic monomer having an alkyl group with a carbon number of 1 to 14. Specifically, Preferably, one or more polymers from the group consisting of ethylhexyl acrylate, butyl acrylate, ethyl acrylate, methyl acrylate, acrylic acid, hydroxyethyl acrylate and hydroxybutyl acrylate can be selected. It may be a polymer containing monomers polymerized, including monomers bonded to a carboxyl group or a hydroxyl group.

並且,用於形成第一黏結層10的黏結組合物還可包括光聚合引發劑及交聯劑,只要是在本技術領域中通常使用的,沒有特別限定。 Furthermore, the adhesive composition used to form the first adhesive layer 10 may also include a photopolymerization initiator and a cross-linking agent, which are not particularly limited as long as they are commonly used in this technical field.

上述交聯劑起到增加黏結組合物的凝聚力的作用,可混合使用一種以上的交聯劑,例如,異氰酸酯類交聯劑、環氧類交聯劑、氮丙啶類交聯劑及金屬螯合物類交聯劑等。 The above-mentioned cross-linking agents play a role in increasing the cohesion of the adhesive composition, and more than one cross-linking agent can be mixed and used, for example, isocyanate cross-linking agents, epoxy cross-linking agents, aziridine cross-linking agents and metal chelates Compound cross-linking agents, etc.

上述光聚合引發劑作為通過紫外線照射來引發紫外線固化交聯劑的反應的物質,考慮樹脂組合物的固化速度等,適當選擇其種類和含量並使用,可通過混合一種以上的光聚合引發劑來使用。 例如,可使用羥基環己基苯基酮(hydroxycyclohexylphenylketone;Irgacure 184)、2-甲基-1-[4-(甲硫基)苯基]-2-嗎啉基-丙烷-1-酮(2-methyl-1[4-(methythio)phenyl]-2-morpholino-propan-1-on;Irgacure 907)、α,α-甲氧基-α-羥基苯乙酮(α,α-methoxy-αhydroxyacetophenone;Irgacure 651)及2-羥基-2-甲基-1-苯基丙烷-1-酮(2-hydroxy-2-methyl-1-phenyl-propan-1-one;Irgacure 1173)等。 The above-mentioned photopolymerization initiator is a substance that initiates the reaction of the ultraviolet curing cross-linking agent by ultraviolet irradiation. The type and content of the photopolymerization initiator are appropriately selected and used in consideration of the curing speed of the resin composition. It can be obtained by mixing one or more photopolymerization initiators. use. For example, hydroxycyclohexylphenylketone (Irgacure 184), 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinyl-propan-1-one (2- methyl-1[4-(methythio)phenyl]-2-morpholino-propan-1-on; Irgacure 907), α,α-methoxy-α-hydroxyacetophenone (α,α-methoxy-αhydroxyacetophenone; Irgacure 651) and 2-hydroxy-2-methyl-1-phenyl-propan-1-one (2-hydroxy-2-methyl-1-phenyl-propan-1-one; Irgacure 1173), etc.

另一方面,對第一黏結層10的厚度沒有特別限定,例如,厚度可以為約10μm~100μm。 On the other hand, the thickness of the first adhesive layer 10 is not particularly limited. For example, the thickness may be about 10 μm ~ 100 μm.

儘管在圖2中未示出,但還可包括設置在第一黏結層的上部面並通過上述第一黏結層黏結的離型膜。可對上述離型膜的一側面進行離型處理。上述離型處理只要是在本領域通常用於離型處理的物質,可不受限制地使用,例如,較佳地,用矽酮進行離型處理。 Although not shown in FIG. 2 , it may also include a release film disposed on the upper surface of the first adhesive layer and bonded through the first adhesive layer. One side of the above-mentioned release film can be subjected to release treatment. The above-mentioned release treatment can be used without restriction as long as it is a substance commonly used for release treatment in this field. For example, preferably, silicone is used for release treatment.

第二黏結層 Second bonding layer

在圖2中,第二黏結層30配置於上部基材層20與下部基材層40之間,在背面研磨製程中作用為可緩和晶圓的衝擊的緩衝層及具有光散射效果的光擴散層。 In FIG. 2 , the second adhesive layer 30 is disposed between the upper base material layer 20 and the lower base material layer 40 , and functions as a buffer layer that can alleviate the impact of the wafer and a light diffusion with light scattering effect during the back grinding process. layer.

像這樣,為了具有緩衝效果,本發明的第二黏結層30的剪切儲能模量越低,越有利,但是當剪切儲能模量過低時,在背面研磨製程中,隨著溫度的上升,可產生緩衝層在高溫中流動或厚度不均勻的問題。考慮到上述問題,較佳地,在30℃的溫度條件下的上述第二黏結層30的剪切儲能模量為0.05MPa~5MPa,更佳地,0.05MPa~3MPa,最佳地,0.05MPa~2.5MPa。本發明的包括第二黏結層30的 晶圓背面研磨用黏結膜100具有對晶圓的表面優秀的緩衝效果,也可在背面研磨製程後提高晶圓的厚度均勻性的優點。 In this way, in order to have a buffering effect, the lower the shear storage modulus of the second adhesive layer 30 of the present invention, the more advantageous it is. However, when the shear storage modulus is too low, during the back grinding process, with the temperature The rise of the buffer layer may cause problems such as flow or uneven thickness of the buffer layer at high temperatures. Considering the above problems, preferably, the shear storage modulus of the second adhesive layer 30 under the temperature condition of 30°C is 0.05MPa~5MPa, more preferably, 0.05MPa~3MPa, most preferably, 0.05 MPa~2.5MPa. The present invention includes the second adhesive layer 30 The adhesive film 100 for wafer back grinding has the advantage of excellent buffering effect on the surface of the wafer, and can also improve the thickness uniformity of the wafer after the back grinding process.

並且,本發明的第二黏結層30可由包含透光性黏結樹脂及光散射粒子P的黏結組合物形成,因此用作賦予光散射效果的光擴散層。通過如上所述的第二黏結層30的光散射效果,為了剝離晶圓背面研磨用黏結膜而照射的能量射線均勻地分散,可減少或抑制剝離時黏結劑殘留物的產生,可優秀地提高工藝性及製備的半導體芯片的品質。並且,用於形成第二黏結層30的黏結組合物可根據需要,混合一種以上的交聯劑使用,如金屬螯合物類交聯劑、異氰酸酯類交聯劑、環氧類交聯劑等。 Furthermore, the second adhesive layer 30 of the present invention can be formed from an adhesive composition including a translucent adhesive resin and light scattering particles P, and therefore serves as a light diffusion layer that provides a light scattering effect. Due to the light scattering effect of the second adhesive layer 30 as described above, the energy rays irradiated for peeling off the adhesive film for back polishing of the wafer are evenly dispersed, thereby reducing or suppressing the generation of adhesive residue during peeling, and excellently improving the Processability and quality of prepared semiconductor chips. Moreover, the adhesive composition used to form the second adhesive layer 30 can be mixed with more than one cross-linking agent as needed, such as metal chelate cross-linking agents, isocyanate cross-linking agents, epoxy cross-linking agents, etc. .

因此,為了使第二黏結層30表現散射效果,通過實驗導出了透光性黏結樹脂及光散射粒子P的折射率的差異較佳為0.05~0.2,這種關係可通過如下式1來具體化。 Therefore, in order to make the second adhesive layer 30 exhibit the scattering effect, it is deduced through experiments that the difference in the refractive index of the translucent adhesive resin and the light scattering particles P is preferably 0.05~0.2. This relationship can be embodied by the following formula 1 .

Figure 111130484-A0305-02-0015-1
Figure 111130484-A0305-02-0015-1

在上述式1中,A是透光性黏結樹脂的折射率,B是光散射粒子的折射率。 In the above formula 1, A is the refractive index of the translucent binder resin, and B is the refractive index of the light scattering particles.

並且,以100重量份的用於形成本發明的第二黏結層30的黏結組合物為基準,較佳地,包含0.1重量份至10重量份的光散射粒子P。若光散射粒子P的含量小於0.1重量份,則光散射效果可能不夠充分。並且,若光散射粒子P的含量大於10重量份,則總透光率降低,在剝離過程中基於能量射線的固化無法進行到需要的程度,減少黏結 劑殘留物的效果可能不充分,由於包含過量粒子可對晶圓背面研磨製程後晶圓的均勻度產生不利的影響。 Furthermore, based on 100 parts by weight of the adhesive composition for forming the second adhesive layer 30 of the present invention, it is preferred to include 0.1 to 10 parts by weight of the light scattering particles P. If the content of the light scattering particles P is less than 0.1 parts by weight, the light scattering effect may not be sufficient. Moreover, if the content of the light scattering particles P is greater than 10 parts by weight, the total light transmittance is reduced, and the curing based on energy rays cannot be performed to the required extent during the peeling process, reducing adhesion. The effectiveness of agent residues may not be sufficient as the inclusion of excess particles may adversely affect the uniformity of the wafer after the wafer back grinding process.

以下,對包含在第二黏結層30的透光性黏結樹脂及光散射粒子P分別進行詳細說明。 Hereinafter, the translucent adhesive resin and the light scattering particles P included in the second adhesive layer 30 will be described in detail.

光散射粒子 light scattering particles

上述光散射粒子P是用於擴散或散射光的粒子,較佳地,具有透光性的透明微粒,只要透光性高,並非一定是無色的,也可以是著色的。並且,為了使光散射效果均勻,較佳地,光散射粒子P具有球體(sphere)的形狀,並且,為了具有高透光性,較佳地,上述光散射粒子P的折射率在1.42~1.60的範圍內。 The above-mentioned light scattering particles P are particles for diffusing or scattering light. Preferably, they are transparent particles with light transmittance. As long as the light transmittance is high, they are not necessarily colorless and may be colored. Furthermore, in order to make the light scattering effect uniform, it is preferable that the light scattering particles P have a sphere shape, and in order to have high light transmittance, it is preferable that the refractive index of the above light scattering particles P is between 1.42 and 1.60. within the range.

並且,上述光散射粒子P的平均粒徑較佳為1μm~50μm,更佳為1μm~10μm。當平均粒徑小於1μm時,光擴散效果或光散射效果低,當大於50μm時,由於粒子過粗,可使得包含其的第二黏結層30及晶圓背面研磨用黏結膜100的厚度均勻度降低。另一方面,上述平均粒徑依據庫爾特計數(coulter counter)法進行測定。雖然為了提高均勻性,較佳地,光散射粒子P的平均粒徑通常是均勻的,但為了調節擴散特性,也可將不同材料或粒徑的2種以上的光散射粒子P混合使用。 Furthermore, the average particle diameter of the light scattering particles P is preferably 1 μm to 50 μm, more preferably 1 μm to 10 μm. When the average particle size is less than 1 μm, the light diffusion effect or light scattering effect is low. When it is larger than 50 μm, the thickness uniformity of the second adhesive layer 30 and the adhesive film 100 for wafer back grinding may be affected because the particles are too coarse. reduce. On the other hand, the above-mentioned average particle diameter is measured based on the coulter counter method. Although in order to improve uniformity, it is preferable that the average particle diameter of the light scattering particles P is usually uniform, in order to adjust the diffusion characteristics, two or more types of light scattering particles P of different materials or particle sizes may be mixed and used.

若能夠滿足如上所述的多個條件,則對光散射粒子P的種類沒有特別限定,可包含無機粒子及有機粒子中的一種以上。上述無機粒子可包含選自由二氧化矽粒子、玻璃粉及石英粒子組成的組中的一種以上。上述有機粒子可包含選自由丙烯酸樹脂粒子、聚苯乙烯 樹脂粒子、苯乙烯-丙烯酸共聚物成分的粒子、聚乙烯樹脂粒子、環氧樹脂粒子、矽樹脂粒子、聚偏氟乙烯粒子、聚四氟乙烯粒子、二乙烯基苯樹脂粒子、苯酚樹脂粒子、氨基甲酸乙酯樹脂粒子、醋酸纖維素粒子、尼龍粒子、纖維素粒子、苯代三聚氰胺樹脂粒子及三聚氰胺樹脂粒子組成的組中的一種以上。 As long as the plurality of conditions described above are satisfied, the type of the light scattering particles P is not particularly limited, and may include at least one type of inorganic particles and organic particles. The inorganic particles may include at least one selected from the group consisting of silica particles, glass powder, and quartz particles. The above-mentioned organic particles may include acrylic resin particles, polystyrene Resin particles, particles of styrene-acrylic copolymer components, polyethylene resin particles, epoxy resin particles, silicone resin particles, polyvinylidene fluoride particles, polytetrafluoroethylene particles, divinylbenzene resin particles, phenol resin particles, One or more types from the group consisting of urethane resin particles, cellulose acetate particles, nylon particles, cellulose particles, benzoguanamine resin particles and melamine resin particles.

透光性黏結樹脂 Translucent adhesive resin

本發明的第二黏結層30為了起到作為光擴散層的功能,形成其的黏結樹脂可選自透光性黏結樹脂。 In order for the second adhesive layer 30 of the present invention to function as a light diffusion layer, the adhesive resin forming the second adhesive layer 30 may be selected from translucent adhesive resins.

例如,較佳地,透光性黏結樹脂的折射率在1.40~1.70的範圍內,更佳地,在1.45~1.55的範圍內。 For example, preferably, the refractive index of the translucent adhesive resin is in the range of 1.40 to 1.70, and more preferably, in the range of 1.45 to 1.55.

上述透光性黏結樹脂只要是具有透光性樹脂材料,如具有透光性的熱塑性樹脂、熱固化樹脂或光固化樹脂等,沒有特別限定。例如,可使用常溫減壓黏結性樹脂,如聚乙烯樹脂、聚丙烯樹脂、環烯烴類樹脂、聚酯類樹脂、環氧類樹脂、聚氨酯類樹脂、矽類樹脂及丙烯酸類樹脂等,或者,也可使用不具有常溫減壓黏結性的樹脂,如聚甲基丙烯酸甲酯樹脂、聚碳酸酯樹脂、聚對苯二甲酸乙二醇酯樹脂及聚氯乙烯樹脂等。 The above-mentioned translucent adhesive resin is not particularly limited as long as it is a translucent resin material, such as translucent thermoplastic resin, thermosetting resin, or photocurable resin. For example, normal temperature pressure-reduced adhesive resins can be used, such as polyethylene resin, polypropylene resin, cycloolefin resin, polyester resin, epoxy resin, polyurethane resin, silicone resin, and acrylic resin, or, Resins that do not have room temperature pressure reduction adhesive properties, such as polymethyl methacrylate resin, polycarbonate resin, polyethylene terephthalate resin, and polyvinyl chloride resin, can also be used.

較佳地,在本發明中,作為透光性黏結樹脂可使用丙烯酸類黏結樹脂。例如,丙烯酸類黏結樹脂可以為丙烯酸類單體的均聚物或共聚物,如丙烯酸及其酯、甲基丙烯酸及其酯、丙烯醯胺及丙烯腈等,並且,可以是上述丙烯酸類單體的至少一種與乙烯基單體的共聚物,如乙酸乙烯酯、馬來酸酐或苯乙烯等。並且,可通過進一步 與選自具有黏結性的單體,如丙烯酸乙酯、丙烯酸丁酯及丙烯酸2-乙基己酯等;用作凝聚力成分的單體,如乙酸乙烯酯、丙烯醯胺、丙烯腈、苯乙烯及甲基丙烯酸酯等;更能提高黏結力的含官能團的單體,如丙烯酸、甲基丙烯酸、衣康酸、馬來酸酐、甲基丙烯酸羥乙酯、甲基丙烯酸羥丙酯、甲基丙烯酸二甲氨基乙酯、羥甲基丙烯醯胺、甲基丙烯酸縮水甘油酯等;用於調節折射率的含氟丙烯酸酯或含硫丙烯酸酯組成的組中的一種以上共聚合來作為丙烯酸類黏結樹脂使用。 Preferably, in the present invention, an acrylic adhesive resin can be used as the translucent adhesive resin. For example, the acrylic adhesive resin can be a homopolymer or copolymer of acrylic monomers, such as acrylic acid and its esters, methacrylic acid and its esters, acrylamide, acrylonitrile, etc., and can be the above-mentioned acrylic monomers. At least one copolymer with a vinyl monomer, such as vinyl acetate, maleic anhydride or styrene. And, by further With monomers selected from the group consisting of adhesive monomers, such as ethyl acrylate, butyl acrylate, and 2-ethylhexyl acrylate, etc.; monomers used as cohesion components, such as vinyl acetate, acrylamide, acrylonitrile, and styrene. and methacrylate, etc.; functional group-containing monomers that can improve adhesion, such as acrylic acid, methacrylic acid, itaconic acid, maleic anhydride, hydroxyethyl methacrylate, hydroxypropyl methacrylate, methyl Dimethylaminoethyl acrylate, hydroxymethylacrylamide, glycidyl methacrylate, etc.; copolymerization of one or more of the group consisting of fluorine-containing acrylates or sulfur-containing acrylates used to adjust the refractive index as acrylics Adhesive resin is used.

另一方面,對第二黏結層30的厚度沒有特別限定,例如,厚度可以為約10μm~100μm。 On the other hand, the thickness of the second adhesive layer 30 is not particularly limited. For example, the thickness may be about 10 μm ~ 100 μm.

晶圓背面研磨用黏結膜 Adhesive film for wafer backside grinding

較佳地,本發明的晶圓背面研磨用黏結膜100的總透光率為70%以上,漫透射率為6%以上。 Preferably, the total light transmittance of the adhesive film 100 for wafer back polishing of the present invention is more than 70%, and the diffuse transmittance is more than 6%.

具體地,為了從晶圓剝離晶圓背面研磨用黏結膜100,為了降低黏結力,通過照射能量射線(典型的是紫外線)來進行固化反應。在此情況下,基於能量射線的固化反應能夠充分地進行,較佳地,總透光率為70%以上。 Specifically, in order to peel off the wafer back polishing adhesive film 100 from the wafer and reduce the adhesive force, a curing reaction is performed by irradiating energy rays (typically ultraviolet rays). In this case, the curing reaction based on energy rays can be fully carried out, and preferably, the total light transmittance is 70% or more.

另一方面,由於本發明的第二黏結層30包含光散射粒子P,光散射或光擴散效果表現在晶圓背面研磨用黏結膜100的整體結構中。像這樣,為了充分地顯示光散射或光擴散效果,較佳地,對晶圓背面研磨用黏結膜100的整體結構的漫透射率為6%以上。 On the other hand, since the second adhesive layer 30 of the present invention includes the light scattering particles P, the light scattering or light diffusion effect is manifested in the overall structure of the adhesive film 100 for wafer back grinding. In order to fully demonstrate the light scattering or light diffusion effect, it is preferable that the diffuse transmittance of the entire structure of the adhesive film 100 for wafer back polishing is 6% or more.

以下,通過本發明的較佳實施例來更詳細地說明本發明的結構及作用。但是,這是作為本發明的較佳示例提出的,並在任 何意義上都不能解釋為限制了本發明。未在此記載的內容只要是本技術領域的通常知識者可充分地在技術上類推,因此省略其說明。 Below, the structure and function of the present invention will be described in more detail through preferred embodiments of the present invention. However, this is presented as a preferred example of the invention and should not be It should not be construed as limiting the invention in any sense. Contents not described here can be fully deduced technically by a person with ordinary knowledge in the technical field, and therefore the description thereof is omitted.

製備例1:用於形成第一黏結層的第一黏結組合物的製備 Preparation Example 1: Preparation of the first adhesive composition for forming the first adhesive layer

將由27克丙烯酸正丁酯(BA)、48克丙烯酸甲酯(MA)及25克丙烯酸羥乙酯(HEA)組成的單體混合物放入反應器中,在反應器中通過設置冷卻裝置來使得氮氣回流且容易調節溫度。 A monomer mixture consisting of 27 grams of n-butyl acrylate (BA), 48 grams of methyl acrylate (MA) and 25 grams of hydroxyethyl acrylate (HEA) was put into the reactor, and a cooling device was set up in the reactor to Nitrogen reflux and easy temperature adjustment.

接下來,相對於100重量份的上述單體混合物,放入作為溶劑的100重量份的乙酸乙酯(EAc),為了去除上述反應器內的氧氣,注入氮氣且在30℃的溫度條件下充分混合30分鐘以上。之後,將溫度上升至50℃並保持,作為反應引發劑放入0.1重量份濃度的偶氮二異丁腈,開始進行反應之後,通過聚合24小時來製備第一反應物。 Next, 100 parts by weight of ethyl acetate (EAc) as a solvent was added to 100 parts by weight of the above-mentioned monomer mixture. In order to remove oxygen in the above-mentioned reactor, nitrogen gas was injected and sufficient temperature was maintained at 30°C. Mix for 30 more minutes. Thereafter, the temperature was raised to 50°C and maintained, and azobisisobutyronitrile with a concentration of 0.1 parts by weight was added as a reaction initiator to start the reaction, and then polymerized for 24 hours to prepare a first reactant.

將24.6重量份的2-甲基丙烯醯氧基乙基異氰酸酯(MOI)及相對於MOI的1重量份的催化劑(二月桂酸二丁基錫(DBTDL:dibutyl tin dilaurate))與上述第一反應物配合,通過在40℃的溫度條件下反應24小時來得到重均分子量為50萬的丙烯酸類黏結樹脂。 24.6 parts by weight of 2-methacryloyloxyethyl isocyanate (MOI) and 1 part by weight of the catalyst (dibutyl tin dilaurate (DBTDL: dibutyl tin dilaurate)) relative to the MOI were combined with the first reactant , an acrylic adhesive resin with a weight average molecular weight of 500,000 was obtained by reacting at a temperature of 40°C for 24 hours.

以100重量份的上述丙烯酸類黏結樹脂為基準,添加作為光聚合引發劑的0.1重量份的Irgacure184(BASF公司)及作為交聯劑的2重量份的異氰酸酯類交聯劑(日本聚氨酯工業株式會社(Nippon Polyurethane Kogyo Co.,Ltd.),商品名“Coronate C”)後,充分混合,製備用於形成第一黏結層的第一黏結組合物。 Based on 100 parts by weight of the above-mentioned acrylic adhesive resin, 0.1 parts by weight of Irgacure 184 (BASF Company) as a photopolymerization initiator and 2 parts by weight of an isocyanate cross-linking agent (Japan Polyurethane Industry Co., Ltd.) as a cross-linking agent were added (Nippon Polyurethane Kogyo Co., Ltd., trade name "Coronate C"), and then mix thoroughly to prepare a first adhesive composition for forming a first adhesive layer.

製備例2:用於形成第二黏結層的第二黏結組合物的製備 Preparation Example 2: Preparation of the second adhesive composition for forming the second adhesive layer

通過將20重量份的丙烯酸丁酯、10重量份的丙烯酸乙基己酯、55重量份的丙烯酸甲酯、7重量份的丙烯酸2-羥乙酯、8重量份的丙烯酸、0.05重量份的偶氮二異丁腈及100重量份的乙酸乙酯進行混合來獲得的混合物,通過在氮氣氣氛及60℃的溫度條件下聚合6小時來得到重均分子量為60萬的丙烯酸類黏結樹脂。 By adding 20 parts by weight of butyl acrylate, 10 parts by weight of ethylhexyl acrylate, 55 parts by weight of methyl acrylate, 7 parts by weight of 2-hydroxyethyl acrylate, 8 parts by weight of acrylic acid, 0.05 parts by weight of even The mixture obtained by mixing nitrogen bisisobutyronitrile and 100 parts by weight of ethyl acetate was polymerized in a nitrogen atmosphere and a temperature of 60° C. for 6 hours to obtain an acrylic adhesive resin with a weight average molecular weight of 600,000.

以100重量份的上述丙烯酸類黏結樹脂為基準,在添加3重量份的異氰酸酯類交聯劑(日本聚氨酯工業株式會社(Nippon Polyurethane Kogyo Co.,Ltd.)製備,商品名“Coronate C”)後,進行充分混合,製備用於形成第二黏結層的第二黏結組合物。 Based on 100 parts by weight of the above-mentioned acrylic adhesive resin, after adding 3 parts by weight of isocyanate cross-linking agent (prepared by Nippon Polyurethane Kogyo Co., Ltd., trade name "Coronate C") , mix thoroughly to prepare a second adhesive composition for forming a second adhesive layer.

上述製備的第二黏結組合物的折射率測定為1.48,在測定時通過使用阿貝(Abbe)折射儀來進行測定。 The refractive index of the second adhesive composition prepared above was measured to be 1.48, and the refractive index was measured by using an Abbe refractometer.

實施例1 Example 1

通過將製備例1的第一黏結組合物塗敷在離型處理的PET(聚對苯二甲酸乙二醇酯膜,厚度為50μm)上,使第一黏結層的厚度達到20μm,通過將50μm厚度的雙向拉伸聚對苯二甲酸乙二醇酯(PET)膜(基材)黏合來製備具有120μm厚度的第一黏結層的第一複合膜。 By coating the first adhesive composition of Preparation Example 1 on the release-treated PET (polyethylene terephthalate film, thickness 50 μm), the thickness of the first adhesive layer reaches 20 μm, and the thickness of the first adhesive layer is reduced to 50 μm. Thick biaxially stretched polyethylene terephthalate (PET) film (substrate) was bonded to prepare a first composite film with a first adhesive layer having a thickness of 120 μm.

接下來,以100重量份的製備例2的第二黏結組合物為基準,添加作為光散射粒子的折射率為1.59、平均粒徑為3μm的1.0重量份的聚苯乙烯成分的有機粒子(稱為“b1”)後,充分混合,並塗敷 在厚度為25μm的雙向拉伸聚對苯二甲酸乙二醇酯(PET)膜上,使得其厚度達到20μm,製備具有厚度為45μm的第二黏結層的第二複合膜。 Next, based on 100 parts by weight of the second adhesive composition of Preparation Example 2, 1.0 parts by weight of polystyrene component organic particles (weighed as light scattering particles) having a refractive index of 1.59 and an average particle diameter of 3 μm were added. For "b1"), mix thoroughly and apply On a biaxially stretched polyethylene terephthalate (PET) film with a thickness of 25 μm, so that the thickness reaches 20 μm, a second composite film having a second adhesive layer with a thickness of 45 μm was prepared.

通過將上述第一複合膜與第二複合膜接合來製備整體厚度為115μm(整體厚度不包括離開型PET的厚度)的晶圓背面研磨用黏結膜。 An adhesive film for wafer backside polishing with an overall thickness of 115 μm (the overall thickness does not include the thickness of the release-type PET) was prepared by joining the first composite film and the second composite film.

實施例2及實施例3及比較例1至比較例3 Example 2 and Example 3 and Comparative Examples 1 to 3

在實施例1中,除了將各成分的種類或含量、黏結層的厚度等變更為如下表1,通過與實施例1相同的方式分別製備了晶圓背面研磨用黏結膜。 In Example 1, an adhesive film for wafer backside polishing was prepared in the same manner as in Example 1, except that the type or content of each component, the thickness of the adhesive layer, etc. were changed to Table 1 below.

實驗例1:光特性評價 Experimental Example 1: Optical Characteristics Evaluation

相對於上述實施例1至實施例3及比較例1至比較例3的晶圓背面研磨用黏結膜,通過利用混濁度測量儀(hazemeter)設備(Nippon Denshoku公司,NDH5000)來測定整體透射率(T.T,%)及漫透射率(D.T,%),將其結構顯示在表1中。 With respect to the adhesive films for wafer back polishing of Examples 1 to 3 and Comparative Examples 1 to 3, the overall transmittance ( T.T, %) and diffuse transmittance (D.T, %), and its structure is shown in Table 1.

實驗例2:測定第二黏結層的剪切儲能模量 Experimental Example 2: Determination of the Shear Storage Modulus of the Second Adhesive Layer

使用作為剪切儲能模量測定裝置的流變儀(Rheometer,TA instruments公司;ARES-G2),將通過層疊由用於形成上述實施例1至實施例3及比較例1至比較例3的晶圓背面研磨用黏結膜的第二黏結層的第二黏結組合物溶液形成的單層黏結層來得到尺寸為直徑8mm×厚度1mm的樣品,將在1Hz從-20℃至120℃的溫度環境下測定剪切儲能模量,在30℃的溫度條件下記錄剪切儲能模量,並顯示在如下的表1中。 Using a rheometer (Rheometer, TA Instruments; ARES-G2) as a shear storage modulus measuring device, the materials used to form the above-described Examples 1 to 3 and Comparative Examples 1 to 3 were stacked. The wafer backside is ground to obtain a single-layer adhesive layer formed by the second adhesive composition solution of the second adhesive layer of the adhesive film to obtain a sample with a size of 8 mm in diameter × 1 mm in thickness, and the temperature environment is from -20°C to 120°C at 1Hz. The shear storage modulus was measured at a temperature of 30°C and recorded in Table 1 below.

實驗例3:晶圓背面研磨後厚度均勻度及殘留物測試 Experimental Example 3: Thickness uniformity and residue test after wafer backside grinding

將上述實施例1至實施例3及比較例1至比較例3的晶圓背面研磨用黏結膜黏附於半導體電路面(=晶圓表面)後,使用背面研磨設備(DISCO公司;DGP8760),對厚度為725μm的晶圓進行背面研磨至厚度為100μm。 After the adhesive films for wafer back polishing in Examples 1 to 3 and Comparative Examples 1 to 3 were adhered to the semiconductor circuit surface (= wafer surface), back polishing equipment (DISCO; DGP8760) was used. Wafers with a thickness of 725 μm were back ground to a thickness of 100 μm.

在背面研磨製程結束後,利用曝光設備(世明VACTRON;TRSJ-3000)照射300mJ/cm2的紫外線A。然後,將熱封膠帶(Heat Sealing tape;MBS-100R)在220℃的溫度條件下熱壓接在晶圓背面研磨用黏結膜的一側外圍部後,去除晶圓背面研磨用黏結膜。 After the back grinding process is completed, the exposure equipment (Shiming VACTRON; TRSJ-3000) is used to irradiate 300mJ/cm2 of ultraviolet A. Then, heat sealing tape (MBS-100R) is thermocompressed on one side of the peripheral portion of the adhesive film for wafer back polishing under a temperature condition of 220°C, and then the adhesive film for wafer back polishing is removed.

在背面研磨製程後,通過顯微鏡觀察去除黏結膜的晶圓表面的20個點來確認晶圓的厚度均勻度及是否產生黏結劑殘留物,具體的方法如下。 After the back grinding process, observe 20 points on the wafer surface with the adhesive film removed through a microscope to confirm the thickness uniformity of the wafer and whether adhesive residue is produced. The specific method is as follows.

1.黏結劑殘留物測試 1. Adhesive residue testing

測定在背面研磨的晶圓內的20個點的殘留物的大小,如下進行評價,並將其結果顯示在如下的表1中。 The size of the residues at 20 points in the back-polished wafer was measured and evaluated as follows. The results are shown in Table 1 below.

○:沒有大小為10μm以下的殘留物 ○: No residue with a size of 10 μm or less

△:產生大小為10μm以下的殘留物 △: Residues with a size of 10 μm or less are generated

×:大量產生大小為10μm以上的殘留物 ×: Residues with a size of 10 μm or more are produced in large quantities

2.晶圓的厚度均勻度測試 2. Wafer thickness uniformity test

當在背面研磨的晶圓內的20個點的厚度的標準差為±4μm以下時,將晶圓的厚度均勻度程度評價為良好(○),當厚度標 準差為±6μm以上時,將晶圓的厚度均勻度程度評價為不良(×),並將其結構顯示在如下的表1中。 When the standard deviation of the thickness of 20 points in the back-ground wafer is ±4 μm or less, the thickness uniformity of the wafer is evaluated as good (○). When the tolerance is ±6 μm or more, the thickness uniformity of the wafer is evaluated as poor (×), and its structure is shown in Table 1 below.

Figure 111130484-A0305-02-0023-2
Figure 111130484-A0305-02-0023-2

上述表1的b1至b3如下。 b1 to b3 of the above-mentioned Table 1 are as follows.

-b1:作為光散射粒子,折射率為1.59的聚苯乙烯成分,平均粒徑為3μm。 -b1: As light scattering particles, the polystyrene component has a refractive index of 1.59 and an average particle diameter of 3 μm.

-b2:作為光散射粒子,折射率為1.42的聚四氟乙烯成分,平均粒徑為3μm。 -b2: As light scattering particles, the polytetrafluoroethylene component has a refractive index of 1.42 and an average particle diameter of 3 μm.

-b3:作為光散射粒子,折射率為1.49的聚甲基丙烯酸甲酯成分,平均粒徑為3μm。 -b3: As light scattering particles, the polymethyl methacrylate component has a refractive index of 1.49 and an average particle diameter of 3 μm.

從上述表1中可知,在本發明實施例1至實施例3中,第二黏結層起到緩衝層的功能,在晶圓背面研磨時具有保護效果,同時通過在第二黏結層中包含光散射粒子來在黏結劑殘留物測試及厚度均勻度測試中也顯示出優秀的結果。 It can be seen from the above Table 1 that in Embodiment 1 to Embodiment 3 of the present invention, the second adhesive layer functions as a buffer layer and has a protective effect during back grinding of the wafer. At the same time, by including light in the second adhesive layer Scattering particles also show excellent results in adhesive residue testing and thickness uniformity testing.

相反,比較例1中的第二黏結層中不包含光散射粒子,在黏結劑殘留物測試中大量產生10μm以上大小的殘留物。比較例2中包含過量光散射粒子,在黏結劑殘留物測試及厚度均勻度測試中也顯示不良結果,第二黏結層的剪切儲能模量相對於實施例高。比較例3中的用於形成黏結層的黏結樹脂與光散射粒子的折射率差異過低,由於不滿足式1,因此光散射(擴散)效果不充分,在黏結劑殘留物測試結果中產生10μm以下大小的殘留物,從而抑制殘留物產生效果不理想。 In contrast, the second adhesive layer in Comparative Example 1 did not contain light scattering particles, and a large amount of residues with a size of 10 μm or more were generated in the adhesive residue test. Comparative Example 2 contains excessive light scattering particles and also shows poor results in the adhesive residue test and thickness uniformity test. The shear storage modulus of the second adhesive layer is higher than that of the Example. In Comparative Example 3, the difference in refractive index between the adhesive resin used to form the adhesive layer and the light scattering particles is too low. Since Formula 1 is not satisfied, the light scattering (diffusion) effect is insufficient, resulting in 10 μm in the adhesive residue test results. The effect of inhibiting the generation of residues is unsatisfactory due to residues of the following sizes.

如上所述,雖然參照例示的附圖對本發明進行了說明,但本發明並不受在本說明書中公開的實施例和附圖的限制,顯而易見的是,通常知識者可在本發明的技術思想的範圍內實現多種變形。而且,即使在先說明本發明實施例時沒有明確記載說明對本發明的結構的作用效果,但也應該認可能夠通過相應結構預測的效果。 As described above, although the present invention has been described with reference to the illustrative drawings, the present invention is not limited to the embodiments and drawings disclosed in this specification. It is obvious that a person of ordinary skill can understand the technical idea of the present invention. A variety of deformations can be achieved within the range. Furthermore, even if the effects of the structure of the present invention are not explicitly described in the first description of the embodiments of the present invention, it should be recognized that the effects can be predicted by the corresponding structure.

100:晶圓背面研磨用黏結膜 100: Adhesive film for wafer backside grinding

10:第一黏結層 10: First adhesive layer

20:上部基材層 20: Upper base material layer

30:第二黏結層 30:Second adhesive layer

40:下部基材層 40: Lower base material layer

P:光散射粒子 P: light scattering particles

Claims (13)

一種晶圓背面研磨用黏結膜,其中,包括:多層基材,包括上部基材層及下部基材層;第一黏結層,配置於該上部基材層上;以及第二黏結層,配置於該上部基材層與該下部基材層之間,該第二黏結層由包含透光性黏結樹脂及光散射粒子的黏結組合物形成,並滿足如下式1,該光散射粒子的折射率為1.42~1.60:
Figure 111130484-A0305-02-0026-8
,在該式1中,A是透光性黏結樹脂的折射率,B是光散射粒子的折射率,其中,相對於100重量份的該第二黏結層的該黏結組合物,包含0.1重量份至10重量份的該光散射粒子。
An adhesive film for wafer backside grinding, which includes: a multi-layer base material, including an upper base material layer and a lower base material layer; a first adhesive layer disposed on the upper base material layer; and a second adhesion layer disposed on Between the upper base material layer and the lower base material layer, the second adhesive layer is formed of an adhesive composition including a translucent adhesive resin and light scattering particles, and satisfies the following formula 1. The refractive index of the light scattering particles 1.42~1.60:
Figure 111130484-A0305-02-0026-8
, in the formula 1, A is the refractive index of the translucent adhesive resin, and B is the refractive index of the light scattering particles, wherein, relative to 100 parts by weight of the adhesive composition of the second adhesive layer, 0.1 part by weight is included. to 10 parts by weight of the light scattering particles.
如請求項1之晶圓背面研磨用黏結膜,其中,總透光率為70%以上。 For example, the adhesive film for wafer backside grinding in claim 1 has a total light transmittance of more than 70%. 如請求項1之晶圓背面研磨用黏結膜,其中,漫透射率為6%以上。 For example, the adhesive film for wafer backside grinding according to claim 1, wherein the diffuse transmittance is more than 6%. 如請求項1之晶圓背面研磨用黏結膜,其中,該光散射粒子包含無機粒子及有機粒子中的一種以上。 As claimed in claim 1, the adhesive film for wafer backside polishing, wherein the light scattering particles include at least one of inorganic particles and organic particles. 如請求項1之晶圓背面研磨用黏結膜,其中,該光散射粒子的平均粒徑為1μm~50μm。 For example, the adhesive film for wafer backside grinding according to claim 1, wherein the average particle size of the light scattering particles is 1 μm ~ 50 μm. 如請求項4之晶圓背面研磨用黏結膜,其中,該無機粒子包含選自由二氧化矽粒子、玻璃粉及石英粒子組成的群組中的一種以上。 An adhesive film for wafer backside grinding according to claim 4, wherein the inorganic particles include at least one selected from the group consisting of silicon dioxide particles, glass powder and quartz particles. 如請求項4之晶圓背面研磨用黏結膜,其中,該有機粒子包含選自由丙烯酸樹脂粒子、聚苯乙烯樹脂粒子、苯乙烯-丙烯酸共聚物成分的粒子、聚乙烯樹脂粒子、環氧樹脂粒子、矽樹脂粒子、聚偏氟乙烯粒子、聚四氟乙烯粒子、二乙烯基苯樹脂粒子、苯酚樹脂粒子、氨基甲酸乙酯樹脂粒子、醋酸纖維素粒子、尼龍粒子、纖維素粒子、苯代三聚氰胺樹脂粒子及三聚氰胺樹脂粒子組成的群組中的一種以上。 Such as the adhesive film for wafer backside polishing in claim 4, wherein the organic particles include particles selected from the group consisting of acrylic resin particles, polystyrene resin particles, styrene-acrylic acid copolymer components, polyethylene resin particles, and epoxy resin particles. , silicone resin particles, polyvinylidene fluoride particles, polytetrafluoroethylene particles, divinylbenzene resin particles, phenol resin particles, urethane resin particles, cellulose acetate particles, nylon particles, cellulose particles, benzomelamine One or more of the group consisting of resin particles and melamine resin particles. 如請求項1之晶圓背面研磨用黏結膜,其中,該第一黏結層的厚度為10μm~100μm,該第二黏結層的厚度為10μm~100μm。 For example, the adhesive film for wafer backside grinding of claim 1, wherein the thickness of the first adhesive layer is 10 μm ~ 100 μm, and the thickness of the second adhesive layer is 10 μm ~ 100 μm. 如請求項1之晶圓背面研磨用黏結膜,其中,該下部基材層及該上部基材層分別包含選自由聚對苯二甲酸乙二醇酯、聚萘二甲酸乙二醇酯、聚對苯二甲酸丁二酯、全芳族聚酯、聚醯亞胺、聚醯胺、聚碳酸酯、聚縮醛、改性聚苯醚、聚苯硫醚、聚碸、聚醚酮及雙向拉伸聚丙烯組成的群組中的一種以上。 The adhesive film for wafer backside grinding according to claim 1, wherein the lower base material layer and the upper base material layer respectively comprise polyethylene terephthalate, polyethylene naphthalate, polyethylene naphthalate, Butylene terephthalate, fully aromatic polyester, polyimide, polyamide, polycarbonate, polyacetal, modified polyphenylene ether, polyphenylene sulfide, polystyrene, polyetherketone and bidirectional More than one member of the group consisting of stretched polypropylene. 如請求項9之晶圓背面研磨用黏結膜,其中,該下部基材層及該上部基材層由聚對苯二甲酸乙二醇酯形成。 The adhesive film for wafer backside grinding according to claim 9, wherein the lower base material layer and the upper base material layer are formed of polyethylene terephthalate. 如請求項1之晶圓背面研磨用黏結膜,其中,該第一黏結層由包含丙烯酸類黏結樹脂的黏結組合物形成。 The adhesive film for wafer backside grinding according to claim 1, wherein the first adhesive layer is formed of an adhesive composition containing an acrylic adhesive resin. 如請求項1之晶圓背面研磨用黏結膜,其中,該第二黏結層的該透光性黏結樹脂包含透光性丙烯酸類黏結樹脂。 The adhesive film for wafer backside grinding according to claim 1, wherein the translucent adhesive resin of the second adhesive layer includes a translucent acrylic adhesive resin. 如請求項1之晶圓背面研磨用黏結膜,其中,在30℃的溫度條件下的上述第二黏結層的剪切儲能模量為0.05MPa~5.00MPa。 For example, in the adhesive film for wafer backside grinding of claim 1, the shear storage modulus of the second adhesive layer under a temperature condition of 30°C is 0.05MPa~5.00MPa.
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